Collagen Meniscus Implant XL
K170364 is the FDA 510(k) clearance record for Collagen Meniscus Implant XL, a class II device, cleared for Ivy Sports Medicine, LLC on under FDA product code OLC (Scaffold, Partial Medial Meniscal Defects Extending Into The Red/White Zone, Resorbable Bovine Collagen). FDA's definition for product code OLC reads: "Intended for use in surgical procedures for the repair and reinforcement of soft tissue injuries of the medial meniscus. In repairing and reinforcing medial meniscal defects, the patient must have an intact meniscal rim and anterior and...". FDA records list 2 510(k) clearances for Ivy Sports Medicine, LLC, from to . As of , FDA records show no recalls naming K170364.
Clearance record
- Decision date
- Received
- (85 days to decision)
- Product code
- OLC Scaffold, Partial Medial Meniscal Defects Extending Into The Red/White Zone, Resorbable Bovine Collagen
- Regulation
- 21 CFR 878.3300
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Ivy Sports Medicine, LLC 545 Penobscot Dr., Redwood City CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code OLC
Trailing 12 monthsFDA records hold no clearances under product code OLC in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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